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Analysis of Rare Variant c.2395C>T (p.Arg799Trp) in Gene ERCC4 in Breast Cancer Patients from Bashkortostan
The ERCC4 / FANCQ gene is a potential candidate gene for susceptibility to hereditary breast cancer, being a participant of the Fanconi anemia (FA)/BRCA pathway required for DNA repair. ERCC4 encodes XPF endonuclease which mainly participates in nucleotide excision repair (NER) and interstrand cross...
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Published in: | Russian journal of genetics 2020-05, Vol.56 (5), p.627-632 |
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creator | Bermisheva, M. A. Gilyazova, I. R. Zinnatullina, G. F. Khusnutdinova, E. K. |
description | The
ERCC4
/
FANCQ
gene is a potential candidate gene for susceptibility to hereditary breast cancer, being a participant of the Fanconi anemia (FA)/BRCA pathway required for DNA repair.
ERCC4
encodes XPF endonuclease which mainly participates in nucleotide excision repair (NER) and interstrand crosslink (ICL) repair. Heterozygous mutations in
ERCC4
have been identified in various cancers. In this study the heterozygous mutation c.2395C>T (p.Arg799Trp) in
ERCC4
was found in a hereditary breast cancer patient using next-generation sequencing. Further screening for the
ERCC4
*p.Arg799Trp mutation in 966 breast cancer patients and 686 control individuals revealed heterozygous mutation carriers in both groups, but no statistically significant differences in the frequency of the mutant allele between the two samples were found. The results of our study suggest that the
ERCC4
*p.Arg799Trp mutation is not associated with high risk of breast cancer, although further studies are needed to evaluate the clinical significance of this mutation. |
doi_str_mv | 10.1134/S1022795420050026 |
format | article |
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ERCC4
/
FANCQ
gene is a potential candidate gene for susceptibility to hereditary breast cancer, being a participant of the Fanconi anemia (FA)/BRCA pathway required for DNA repair.
ERCC4
encodes XPF endonuclease which mainly participates in nucleotide excision repair (NER) and interstrand crosslink (ICL) repair. Heterozygous mutations in
ERCC4
have been identified in various cancers. In this study the heterozygous mutation c.2395C>T (p.Arg799Trp) in
ERCC4
was found in a hereditary breast cancer patient using next-generation sequencing. Further screening for the
ERCC4
*p.Arg799Trp mutation in 966 breast cancer patients and 686 control individuals revealed heterozygous mutation carriers in both groups, but no statistically significant differences in the frequency of the mutant allele between the two samples were found. The results of our study suggest that the
ERCC4
*p.Arg799Trp mutation is not associated with high risk of breast cancer, although further studies are needed to evaluate the clinical significance of this mutation.</description><identifier>ISSN: 1022-7954</identifier><identifier>EISSN: 1608-3369</identifier><identifier>DOI: 10.1134/S1022795420050026</identifier><language>eng</language><publisher>Moscow: Pleiades Publishing</publisher><subject>Animal Genetics and Genomics ; Biomedical and Life Sciences ; Biomedicine ; Human Genetics ; Microbial Genetics and Genomics</subject><ispartof>Russian journal of genetics, 2020-05, Vol.56 (5), p.627-632</ispartof><rights>Pleiades Publishing, Inc. 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c240t-c8f263783820212f1f0c8df9e39b46e4e521ffcee36152947840f4e4ccd809ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Bermisheva, M. A.</creatorcontrib><creatorcontrib>Gilyazova, I. R.</creatorcontrib><creatorcontrib>Zinnatullina, G. F.</creatorcontrib><creatorcontrib>Khusnutdinova, E. K.</creatorcontrib><title>Analysis of Rare Variant c.2395C>T (p.Arg799Trp) in Gene ERCC4 in Breast Cancer Patients from Bashkortostan</title><title>Russian journal of genetics</title><addtitle>Russ J Genet</addtitle><description>The
ERCC4
/
FANCQ
gene is a potential candidate gene for susceptibility to hereditary breast cancer, being a participant of the Fanconi anemia (FA)/BRCA pathway required for DNA repair.
ERCC4
encodes XPF endonuclease which mainly participates in nucleotide excision repair (NER) and interstrand crosslink (ICL) repair. Heterozygous mutations in
ERCC4
have been identified in various cancers. In this study the heterozygous mutation c.2395C>T (p.Arg799Trp) in
ERCC4
was found in a hereditary breast cancer patient using next-generation sequencing. Further screening for the
ERCC4
*p.Arg799Trp mutation in 966 breast cancer patients and 686 control individuals revealed heterozygous mutation carriers in both groups, but no statistically significant differences in the frequency of the mutant allele between the two samples were found. The results of our study suggest that the
ERCC4
*p.Arg799Trp mutation is not associated with high risk of breast cancer, although further studies are needed to evaluate the clinical significance of this mutation.</description><subject>Animal Genetics and Genomics</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Human Genetics</subject><subject>Microbial Genetics and Genomics</subject><issn>1022-7954</issn><issn>1608-3369</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kD1PwzAQhi0EEqXwA9g8wpBy_khiL0htVApSJVAprJFxzyX9cCrbHfrvSVU2JKa70_s-NzyE3DIYMCbkwzsDzkudSw6QA_DijPRYASoTotDn3d7F2TG_JFcxrgAYQCF6ZD30ZnOITaStozMTkH6a0BifqB1wofPqcU7vdoNhWJZaz8PunjaeTtAjHc-qSh6vUUATE62Mtxjom0kN-hSpC-2Wjkz8XrchtTEZf00unNlEvPmdffLxNJ5Xz9n0dfJSDaeZ5RJSZpXjhSiVUBw44445sGrhNAr9JQuUmHPmnEUUBcu5lqWS4CRKaxcKtLGiT9jprw1tjAFdvQvN1oRDzaA-2qr_2OoYfmJi1_VLDPWq3YfOTfwH-gEqEmkQ</recordid><startdate>20200501</startdate><enddate>20200501</enddate><creator>Bermisheva, M. A.</creator><creator>Gilyazova, I. R.</creator><creator>Zinnatullina, G. F.</creator><creator>Khusnutdinova, E. K.</creator><general>Pleiades Publishing</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20200501</creationdate><title>Analysis of Rare Variant c.2395C>T (p.Arg799Trp) in Gene ERCC4 in Breast Cancer Patients from Bashkortostan</title><author>Bermisheva, M. A. ; Gilyazova, I. R. ; Zinnatullina, G. F. ; Khusnutdinova, E. K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c240t-c8f263783820212f1f0c8df9e39b46e4e521ffcee36152947840f4e4ccd809ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animal Genetics and Genomics</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Human Genetics</topic><topic>Microbial Genetics and Genomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bermisheva, M. A.</creatorcontrib><creatorcontrib>Gilyazova, I. R.</creatorcontrib><creatorcontrib>Zinnatullina, G. F.</creatorcontrib><creatorcontrib>Khusnutdinova, E. K.</creatorcontrib><collection>CrossRef</collection><jtitle>Russian journal of genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bermisheva, M. A.</au><au>Gilyazova, I. R.</au><au>Zinnatullina, G. F.</au><au>Khusnutdinova, E. K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Analysis of Rare Variant c.2395C>T (p.Arg799Trp) in Gene ERCC4 in Breast Cancer Patients from Bashkortostan</atitle><jtitle>Russian journal of genetics</jtitle><stitle>Russ J Genet</stitle><date>2020-05-01</date><risdate>2020</risdate><volume>56</volume><issue>5</issue><spage>627</spage><epage>632</epage><pages>627-632</pages><issn>1022-7954</issn><eissn>1608-3369</eissn><abstract>The
ERCC4
/
FANCQ
gene is a potential candidate gene for susceptibility to hereditary breast cancer, being a participant of the Fanconi anemia (FA)/BRCA pathway required for DNA repair.
ERCC4
encodes XPF endonuclease which mainly participates in nucleotide excision repair (NER) and interstrand crosslink (ICL) repair. Heterozygous mutations in
ERCC4
have been identified in various cancers. In this study the heterozygous mutation c.2395C>T (p.Arg799Trp) in
ERCC4
was found in a hereditary breast cancer patient using next-generation sequencing. Further screening for the
ERCC4
*p.Arg799Trp mutation in 966 breast cancer patients and 686 control individuals revealed heterozygous mutation carriers in both groups, but no statistically significant differences in the frequency of the mutant allele between the two samples were found. The results of our study suggest that the
ERCC4
*p.Arg799Trp mutation is not associated with high risk of breast cancer, although further studies are needed to evaluate the clinical significance of this mutation.</abstract><cop>Moscow</cop><pub>Pleiades Publishing</pub><doi>10.1134/S1022795420050026</doi><tpages>6</tpages></addata></record> |
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language | eng |
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source | Springer Nature |
subjects | Animal Genetics and Genomics Biomedical and Life Sciences Biomedicine Human Genetics Microbial Genetics and Genomics |
title | Analysis of Rare Variant c.2395C>T (p.Arg799Trp) in Gene ERCC4 in Breast Cancer Patients from Bashkortostan |
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